DIK — Thin Layer Chromatography, Quinine Class I

FDA Device Classification

FDA product code DIK covers "Thin Layer Chromatography, Quinine", a Class I medical device regulated under 21 CFR 862.3750. Submissions are reviewed by the Clinical Toxicology panel.

Classification Details

Product Code
DIK
Device Class
Class I
Regulation Number
862.3750
Submission Type
Review Panel
TX
Medical Specialty
Clinical Toxicology
Implant
No